Variant report

Variant	rs10756742
Chromosome Location	chr9:16049260-16049261
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs1014307	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10733306	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10733307	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10738420	0.81[AMR][1000 genomes]
rs10738422	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10738423	0.83[EUR][1000 genomes]
rs10738424	0.85[EUR][1000 genomes]
rs10738425	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10738426	0.87[CHB][hapmap];0.84[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10738427	0.88[CHB][hapmap];0.85[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10738428	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10738430	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10756728	0.81[AMR][1000 genomes]
rs10756729	0.81[AMR][1000 genomes]
rs10756731	0.81[AMR][1000 genomes]
rs10756733	0.93[AFR][1000 genomes]
rs10756734	0.81[EUR][1000 genomes]
rs10756735	0.94[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs10756736	0.85[EUR][1000 genomes]
rs10756737	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10756739	0.85[EUR][1000 genomes]
rs10756741	0.88[CHB][hapmap];0.85[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10810514	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs10810517	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10810518	0.85[EUR][1000 genomes]
rs10810519	0.83[EUR][1000 genomes]
rs10810520	0.84[EUR][1000 genomes]
rs10810521	0.85[EUR][1000 genomes]
rs10810522	0.85[EUR][1000 genomes]
rs10810523	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10810524	0.85[EUR][1000 genomes]
rs10810526	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10810527	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10810528	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10962256	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10962260	0.86[CHB][hapmap];0.85[JPT][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11788695	0.84[EUR][1000 genomes]
rs12379466	0.85[EUR][1000 genomes]
rs1328273	0.83[AMR][1000 genomes]
rs1328275	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1328276	0.85[EUR][1000 genomes]
rs1328277	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1328278	0.85[EUR][1000 genomes]
rs1328279	0.85[EUR][1000 genomes]
rs1328280	0.85[EUR][1000 genomes]
rs1328296	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1328298	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1359954	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1359956	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1359957	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1410450	0.85[EUR][1000 genomes]
rs1410451	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1410452	0.88[CHB][hapmap];0.80[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1410453	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs1410454	0.87[CHB][hapmap];0.90[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1410455	0.88[CHB][hapmap];0.80[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1887666	0.85[EUR][1000 genomes]
rs1887667	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1887668	0.85[EUR][1000 genomes]
rs1887669	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2026661	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2149233	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2382551	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3824502	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs4247294	0.84[EUR][1000 genomes]
rs4740629	0.81[AMR][1000 genomes]
rs4740631	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4740632	0.84[EUR][1000 genomes]
rs4741557	0.84[EUR][1000 genomes]
rs4741558	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4741559	0.88[CHB][hapmap];0.85[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4741560	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4741561	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7040690	0.81[CHB][hapmap];0.81[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs752489	0.85[EUR][1000 genomes]
rs752490	0.85[EUR][1000 genomes]
rs7873925	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs943787	0.85[EUR][1000 genomes]
rs943788	0.85[EUR][1000 genomes]
rs943789	0.85[EUR][1000 genomes]
rs9792412	0.82[EUR][1000 genomes]
rs997410	0.88[CHB][hapmap];0.85[JPT][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv892637	chr9:15926508-16060746	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv949463	chr9:15970668-16377360	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv831521	chr9:15974174-16106565	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1025555	chr9:16022186-16064158	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv2761506	chr9:16040491-16093736	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16030800-16050000	Weak transcription	Aorta	Aorta
2	chr9:16040600-16057600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:16041200-16049600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:16045400-16057600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr9:16045600-16052200	Weak transcription	Fetal Muscle Leg	muscle
6	chr9:16045600-16057600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr9:16045800-16061000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr9:16046000-16058200	Weak transcription	Fetal Kidney	kidney
9	chr9:16048200-16052200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:16048600-16071400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr9:16049000-16049400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links